Canonical Allele Identifier: CA12938054
Gene: EPHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27595330G>A , CM000670.2:g.27595330G>A GRCh38
NC_000008.10:g.27452847G>A , CM000670.1:g.27452847G>A GRCh37
NC_000008.9:g.27508764G>A NCBI36
NG_027845.1:g.24481C>T

Transcript Alleles

HGVS Amino-acid Change
XR_949609.1:n.3190-1737G>A
XR_949610.1:n.2503-1737G>A
XR_949611.1:n.3149-1737G>A
XR_001745491.1:n.1928-1737G>A